Transition Metal-(μ-Cl)-Aluminum Bonding in α-Olefin and Diene Chemistry.

Autor: Nifant'ev IE; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences (RAS), 29 Leninsky Pr., 119991 Moscow, Russia.; Chemistry Department, M.V. Lomonosov Moscow State University, 1-3 Leninskie Gory, 119991 Moscow, Russia., Salakhov II; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences (RAS), 29 Leninsky Pr., 119991 Moscow, Russia., Ivchenko PV; A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences (RAS), 29 Leninsky Pr., 119991 Moscow, Russia.; Chemistry Department, M.V. Lomonosov Moscow State University, 1-3 Leninskie Gory, 119991 Moscow, Russia.
Jazyk: angličtina
Zdroj: Molecules (Basel, Switzerland) [Molecules] 2022 Oct 23; Vol. 27 (21). Date of Electronic Publication: 2022 Oct 23.
DOI: 10.3390/molecules27217164
Abstrakt: Olefin and diene transformations, catalyzed by organoaluminum-activated metal complexes, are widely used in synthetic organic chemistry and form the basis of major petrochemical processes. However, the role of M−(μ-Cl)−Al bonding, being proven for certain >C=C< functionalization reactions, remains unclear and debated for essentially more important industrial processes such as oligomerization and polymerization of α-olefins and conjugated dienes. Numerous publications indirectly point at the significance of M−(μ-Cl)−Al bonding in Ziegler−Natta and related transformations, but only a few studies contain experimental or at least theoretical evidence of the involvement of M−(μ-Cl)−Al species into catalytic cycles. In the present review, we have compiled data on the formation of M−(μ-Cl)−Al complexes (M = Ti, Zr, V, Cr, Ni), their molecular structure, and reactivity towards olefins and dienes. The possible role of similar complexes in the functionalization, oligomerization and polymerization of α-olefins and dienes is discussed in the present review through the prism of the further development of Ziegler−Natta processes and beyond.
Databáze: MEDLINE
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